DiMiceli Lauren, Pool Vitali, Kelso John M, Shadomy Sean V, Iskander John
Immunization Safety Branch, NIP/CDC, Mail Stop E61, Atlanta, GA 30333, USA.
Vaccine. 2006 Feb 6;24(6):703-7. doi: 10.1016/j.vaccine.2005.07.069. Epub 2005 Aug 9.
The preparation of recombinant hepatitis B vaccines involves using cellular cultures of Saccharomyces cerevisiae, otherwise known as baker's yeast. Prior to vaccine licensure, clinical trials were performed to address whether residual yeast proteins in the vaccines could induce anaphylaxis, including testing for IgE anti-yeast antibody levels. 1-2% of subjects had anti-yeast IgE antibodies before immunization, but demonstrated no significant rise in IgE after HBV. We searched reports in the Vaccine Adverse Event Reporting System (VAERS) for those that mentioned a history of allergy to yeast and then reviewed the adverse events described in these reports for potential anaphylactic reactions. Probable anaphylaxis was defined as the presence of one or more dermatologic symptoms and one or more respiratory, gastrointestinal, or cardiovascular symptoms with onset within 4 h of Hepatitis B vaccination. Possible anaphylaxis was defined in one of two ways: (1) cases that described dermatologic or respiratory symptoms (but not both) occurring within 4h of vaccination; or (2) cases that described one or more dermatologic and/or respiratory symptoms occurring 4-12 h post vaccination. Among the 107 reports of pre-existing "yeast allergies," 11 reports described probable or possible anaphylaxis after HBV. Four additional cases were described after other vaccines. The majority of vaccinees who met the case definitions and had a history of yeast allergies were female, ages ranged from 10 to 64, and symptom onset ranged from 15 min to 5 h after vaccination. No deaths were reported. The small number of reports to VAERS may be partly due to health care professionals observing current contraindications by not vaccinating yeast sensitive individuals. Nevertheless, yeast associated anaphylaxis after HBV in sensitized patients appears to be a rare event.
重组乙型肝炎疫苗的制备涉及使用酿酒酵母的细胞培养物,也就是面包酵母。在疫苗获得许可之前,进行了临床试验,以确定疫苗中的残留酵母蛋白是否会引发过敏反应,包括检测IgE抗酵母抗体水平。1-2%的受试者在免疫前就有抗酵母IgE抗体,但在接种乙肝疫苗后IgE没有显著升高。我们在疫苗不良事件报告系统(VAERS)中搜索了提及酵母过敏史的报告,然后审查了这些报告中描述的不良事件,以寻找潜在的过敏反应。可能的过敏反应定义为在接种乙肝疫苗后4小时内出现一种或多种皮肤症状以及一种或多种呼吸、胃肠道或心血管症状。可能的过敏反应有两种定义方式:(1)描述在接种疫苗后4小时内出现皮肤或呼吸症状(但不是两者都有)的病例;或(2)描述在接种疫苗后4-12小时出现一种或多种皮肤和/或呼吸症状的病例。在107份先前存在“酵母过敏”的报告中,有11份报告描述了接种乙肝疫苗后可能或疑似过敏反应。在接种其他疫苗后又发现了另外4例。大多数符合病例定义且有酵母过敏史的疫苗接种者为女性,年龄在10至64岁之间,症状发作时间在接种疫苗后15分钟至5小时之间。没有死亡报告。向VAERS报告的数量较少,部分原因可能是医护人员遵循当前的禁忌证,不给酵母敏感个体接种疫苗。然而,致敏患者接种乙肝疫苗后与酵母相关的过敏反应似乎是罕见事件。